Kraakman MEM - Search Results

1

A comparison of five Illumina, Ion Torrent, and nanopore sequencing technology-based approaches for whole genome sequencing of SARS-CoV-2.

Carbo EC, Mourik K, Boers SA, Munnink BO, Nieuwenhuijse D, Jonges M, Welkers MRA, Matamoros S, van Harinxma Thoe Slooten J, Kraakman MEM, Karelioti E, van der Meer D, Veldkamp KE, Kroes ACM, Sidorov I, de Vries JJC. Carbo EC, et al. Among authors: kraakman mem. Eur J Clin Microbiol Infect Dis. 2023 Jun;42(6):701-713. doi: 10.1007/s10096-023-04590-0. Epub 2023 Apr 5. Eur J Clin Microbiol Infect Dis. 2023. PMID: 37017810 Free PMC article.

2

Patterns of X chromosome inactivation in haematopoietic cells of female carriers of X linked severe combined immunodeficiency.

Hendriks RW, Kraakman ME, Schuurman RK. Hendriks RW, et al. Immunodeficiency. 1993;4(1-4):263-5. Immunodeficiency. 1993. PMID: 8167715

3

[Early diagnosis in sex-linked agammaglobulinemia].

Post ED, Mensink EJ, Sandkuyl LA, Kraakman ME, van Velzen-Blad H, Schuurman RK. Post ED, et al. Ned Tijdschr Geneeskd. 1987 Oct 31;131(44):1974-7. Ned Tijdschr Geneeskd. 1987. PMID: 2891048 Dutch. No abstract available.

4

Differential methylation at the 5' and the 3' CCGG sites flanking the X chromosomal hypervariable DXS255 locus.

Hendriks RW, Kraakman ME, Mensink RG, Schuurman RK. Hendriks RW, et al. Hum Genet. 1991 Nov;88(1):105-11. doi: 10.1007/BF00204939. Hum Genet. 1991. PMID: 1959916

5

Carrier detection in X-linked immunodeficiencies. II: An X inactivation assay based on differential methylation of a line-1 repeat at the DXS255 locus.

Hinds H, Craig IW, Chen ZY, Kraakman ME, Schuurman RK, Hendriks RW. Hinds H, et al. Immunodeficiency. 1993;4(1-4):213-5. Immunodeficiency. 1993. PMID: 8167703

6

Mutation analysis of the Bruton's tyrosine kinase gene in X-linked agammaglobulinemia: identification of a mutation which affects the same codon as is altered in immunodeficient xid mice.

de Weers M, Mensink RG, Kraakman ME, Schuurman RK, Hendriks RW. de Weers M, et al. Hum Mol Genet. 1994 Jan;3(1):161-6. doi: 10.1093/hmg/3.1.161. Hum Mol Genet. 1994. PMID: 8162018

7

Identification of a novel tumor-specific CTL epitope presented by RMA, EL-4, and MBL-2 lymphomas reveals their common origin.

van Hall T, van Bergen J, van Veelen PA, Kraakman M, Heukamp LC, Koning F, Melief CJ, Ossendorp F, Offringa R. van Hall T, et al. J Immunol. 2000 Jul 15;165(2):869-77. doi: 10.4049/jimmunol.165.2.869. J Immunol. 2000. PMID: 10878361

8

The Bruton's tyrosine kinase gene is expressed throughout B cell differentiation, from early precursor B cell stages preceding immunoglobulin gene rearrangement up to mature B cell stages.

de Weers M, Verschuren MC, Kraakman ME, Mensink RG, Schuurman RK, van Dongen JJ, Hendriks RW. de Weers M, et al. Eur J Immunol. 1993 Dec;23(12):3109-14. doi: 10.1002/eji.1830231210. Eur J Immunol. 1993. PMID: 8258324

9

X-linked immunodeficiency with hyperimmunoglobulinemia M appears to be linked to the DXS42 restriction fragment length polymorphism locus.

Mensink EJ, Thompson A, Sandkuyl LA, Kraakman ME, Schot JD, Espanol T, Schuurman RK. Mensink EJ, et al. Hum Genet. 1987 May;76(1):96-9. doi: 10.1007/BF00283057. Hum Genet. 1987. PMID: 2883112

10

Genetic heterogeneity in X-linked agammaglobulinemia complicates carrier detection and prenatal diagnosis.

Mensink EJ, Thompson A, Schot JD, Kraakman ME, Sandkuyl LA, Schuurman RK. Mensink EJ, et al. Clin Genet. 1987 Feb;31(2):91-6. doi: 10.1111/j.1399-0004.1987.tb02775.x. Clin Genet. 1987. PMID: 2881637

Save citations to file

Email citations

Send citations to clipboard

Add to Collections

Add to My Bibliography

Create a file for external citation management software

Your saved search

Your RSS Feed

My NCBI Filters

Text availability

Article attribute

Article type

Publication date

45 results

Search Page